Asthma Clinical Trial
Official title:
Influence of Probiotics on Prevention of Atopy, Atopic Disease and Immunological Responses- A Randomized Double-Blind Placebo Controlled Trial
This will be a double-blind, randomized placebo-controlled study. 253 children were recruited and randomly assigned into one of 2 groups to receive either normal infant formula or formula with Bifidobacterium longum and Lactobacillus rhamnosus GG. The primary aim is to assess the effect of early administration (from birth) of probiotics on the incidence of allergic sensitization, eczema, asthma and rhinitis.
One of the most important early influences on the immune system is the intestinal
microflora. The gastrointestinal tract, being the largest body area interacting with the
environment, is one of the earliest to be colonized and is quantitatively the most important
source of microbial stimulation for the immature immune system. Probiotics are helpful
bacteria from healthy intestinal tract, and have shown potential in reducing allergy. This
is extremely important as allergic diseases are on the rise worldwide. Probiotics are safe,
easy to administer and can be used early for intervention as allergic sensitization, once
established, is difficult to reverse.
This double-blind, randomized placebo-controlled study has recruited 253 children from
birth. These babies, with a family history of atopic disease, will be randomly assigned into
one of 2 groups to receive either normal infant formula or formula with Bifidobacterium
longum and Lactobacillus rhamnosus GG. The formula will be consumed postnatally for 6
months, after which the child will continue with normal follow-on milk. Children will be
examined at the neonatal period and at 1, 3, 6, 12 and 24 months. Blood samples will be
collected at birth (cord blood) and at 1 year of age. Blood will be analyzed for cytokines,
total IgE and specific IgE. Skin prick test for common allergens will also be performed at 1
year of age. Stools will be collected at 5 days, 1, 3, 12 months and analyzed for the
pattern of stool colonization.
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Caregiver, Investigator), Primary Purpose: Prevention
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